Variant report

Variant rs57343517
Chromosome Location chr1:173894122-173894123
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173856600-173907200 Weak transcription Brain Germinal Matrix brain
2 chr1:173857400-173902000 Weak transcription HSMMtube muscle
3 chr1:173858200-173902800 Weak transcription Left Ventricle heart
4 chr1:173870000-173898000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr1:173871200-173908400 Weak transcription Spleen Spleen
6 chr1:173872400-173896200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:173874400-173899800 Weak transcription Primary T cells from cord blood blood
8 chr1:173879200-173899400 Weak transcription Duodenum Smooth Muscle Duodenum
9 chr1:173882800-173912400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr1:173888400-173900200 Weak transcription Right Atrium heart
11 chr1:173891200-173899400 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr1:173892000-173895200 Weak transcription Stomach Smooth Muscle stomach
13 chr1:173892400-173894400 Enhancers Liver Liver
14 chr1:173893200-173895200 Enhancers Pancreas Pancrea
15 chr1:173893400-173908400 Weak transcription Colonic Mucosa Colon
16 chr1:173894000-173894600 Enhancers Duodenum Mucosa Duodenum
17 chr1:173894000-173896600 Enhancers Fetal Intestine Large intestine
18 chr1:173894000-173897000 Enhancers Fetal Intestine Small intestine
19 chr1:173894000-173904800 Weak transcription Brain Cingulate Gyrus brain

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